15号染色体开放阅读框58抗体

一抗操作步骤：

洗涤：‌洗涤的目的是为了洗去一抗的非特异性结合，‌洗涤的效果直接影响结果背景的深浅。‌建议使用PBST或TBST作为洗涤液，‌其中的Tween20有助于去除非特异性的结合，‌减少背景。‌洗涤的次数和时间根据具体实验来确定，‌建议清洗3-5次，‌每次5分钟。‌

15号染色体开放阅读框58抗体

英文名称：GDPGP1

中文名称：15号染色体开放阅读框58抗体

别    名；C15orf58; Chromosome 15 open reading frame 58; GDP-D-glucose phosphorylase 1; GDP-D-glucose phosphorylase C15orf58; gdpgp1; GDPP1_HUMAN; VTC2.

研究领域；  神经生物学  信号转导  新陈代谢

抗体来源；Rabbit

克隆类型；Polyclonal

交叉反应；Mouse, Rat,  (predicted: Human, Pig, Horse, )

产品应用；WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复）

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

理论分子量；42kDa

细胞定位；细胞浆

性    状；Liquid

浓    度；1mg/ml

免 疫 原；KLH conjugated synthetic peptide derived from human GDPGP1/C15orf58: 301-385/385

亚    型；IgG

纯化方法；affinity purified by Protein A

缓 冲 液；0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存条件；Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

注意事项；This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

产品介绍：

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.

抗体孵育注意事项：‌使用干净的孵育盒子，‌避免油脂等杂物沾到膜上造成非特异信号。‌如果一次性需要检测多个蛋白，‌可以考虑将膜剪开或采用其他技术如抗体洗脱液处理后再次使用膜

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